Insecticide formulations

a technology of insecticide and formulation, which is applied in the field of insecticide formulation, can solve the problems of affecting affecting the survival of insects, and losing the efficacy of most insecticide formulations, especially liquid-based preparations, and achieving the effect of prolonging the effective field life of insecticid

Inactive Publication Date: 2014-12-16
DOW AGROSCIENCES LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Unfortunately, most insecticides formulations, especially liquid-based preparations, lose their efficacy relatively soon after their application.
Additionally, formulations with a short period of post-application activity may result in periods of time during which a surface adjacent to a population of insects is vulnerable to infestation.
This creates a need to periodically apply various insecticidal formulations in order to control continuing pest infestations or to prevent their occurrence, increase the amount of insecticides that must be used, and the increased cost associated with their shipping, handling and application.

Method used

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  • Insecticide formulations
  • Insecticide formulations

Examples

Experimental program
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example 1

Preparation of Insecticidal Formulations

[0045]As illustrated in Table 1, formulations of insecticides, such as chlorpyrifos-methyl, may be incorporated into microcapsules by forming the capsule in the presence of an inert liquid, such as a hydrocarbon fluid and 1-nonanal. Various insecticidal formulations were prepared with different amounts of EDA in a continuous or in-line process as described herein.

[0046]

TABLE 1Example Insecticidal Capsule FormulationsFormulation12811Chlorpyrifos-methyl19.419.419.419.4SOLVESSO ™ 150 ND19.019.019.019.0hydrocarbon fluid1-nonanal0.380.380.380.38PAPI ® 270.62310.62310.62310.6231polymethylenepolyphenylisocyanateEthylenediamine (EDA)0.16040.13950.12560.0977GOHSENOL ® GL031.98861.98861.98861.9886polyvinyl alcoholGEROPON ® SDS0.24480.24480.24480.2448AVICEL ® CL 6110.110.110.110.11stabilizerKELZAN ® ASX0.020.020.020.02xanthan gumPROXEL ® GXL0.050.050.050.05preservativeAntifoam 100 IND0.07560.07560.07560.0756Deionized (DI) water34.734.734.734.7finishing w...

example 2

Evaluation of the Insecticidal Formulations

[0051]Properties of the insecticide formulations formed from the ingredients listed in Table 1 (i.e., formulations 1, 2, 8 and 11) were determined over time. The properties evaluated were pH, particle size, viscosity and syneresis. Such properties were determined immediately after formation (“Initial”). Samples of each of the formulations 1, 2, 8 and 11 were stored at 54° C., 40° C., freezing temperature (FT, about 0° C.) and room temperature (RT, about 25° C.). The properties of the samples stored at 54° C., 40° C., FT and RT were determined after 2 weeks and the properties of the samples stored at 40° C. and RT were determined after 4 weeks. Tables 1 through 5 provide data showing a comparison of each of the properties of formulations 1, 2, 8 and 11 observed after storing each of the formulations as described.

[0052]The pH of the samples of formulations 1, 2, 8 and 11 stored at different temperatures for time periods of 2 weeks and 4 weeks...

example 3

Chlorpyrifos-Methyl Degradation as a Function of Molar Ratio of Aminelsocyanate Groups in the Cross-Linking Amine and Isocyanate Monomer Emulsion Used to Prepare Insecticidal Capsule Formulations

[0061]Degradation of chlorpyrifos-methyl as a function of the molar ratio of amine:isocyanate groups in the cross-linking amine (EDA) and isocyanate monomer (PAPI™ 27) emulsion used to prepare the insecticidal capsule formulations was determined. In each of formulations 1, 2, 8 and 11, an amount of chlorpyrifos-methyl (in wt %) was determined in the samples stored at 54° C., 40° C., freezing temperature (FT, about 0° C.), and room temperature (RT, about 25° C.). The amount of the chlorpyrifos-methyl in each of the formulations was determined immediately after formation of the sample (“Initial”). Additionally, the amount of the chlorpyrifos-methyl in the samples stored at 54° C., 40° C., FT and RT was determined after 2 weeks and the amount of the chlorpyrifos-methyl in the samples stored at ...

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Abstract

Insecticide formulations having improved chemical and physical stability and related methods are disclosed. The insecticide formulations may include a plurality of microcapsules, each including at least one organophosphate insecticide (e.g., chlorpyrifos-methyl) at least partially surrounded by a polymer shell. The insecticide formulations may be used to control insect populations by singular or periodic applications. The microcapsule polymer shell of the insecticide formulations may be formed by combining a cross-linking amine and a hydrophobic monomer (e.g., an isocyanate) at a molar ratio of amine to isocyanate groups of less than about 1:1.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application claims the benefit of U.S. Provisional Patent Application Ser. No. 61 / 442,003, filed Feb. 11, 2011, the disclosure of which is hereby incorporated herein in its entirety by this reference.TECHNICAL FIELD[0002]Various aspects and embodiments relate generally to formulations of insecticide formulations that exhibit advantageous biological, commercial and / or environmental properties.BACKGROUND[0003]Controlling insect population is essential to modern agriculture, food storage, and hygiene. Currently, safe and effective encapsulated insecticidal formulations play a significant role in controlling insect populations. Properties of useful encapsulated insecticidal formulations include good efficacy against targeted pests, including good initial toxicity against targeted insects, ease of handling, stability, advantageous residence times in the environment and, in some instances, a long effective period of insecticidal activity af...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): A01N25/10A01N25/28A01P7/04A01N57/16
CPCA01N57/16A01N25/28A01N2300/00A01N25/26A01N59/26
Inventor WUJEK, DENNIS G.BOUCHER, JR., RAYMOND E.LOGAN, MARTIN C.WILSON, STEPHEN L.LI, MEIAULISA, LORENZO
Owner DOW AGROSCIENCES LLC
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